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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63795Generated: October 30, 2026

4-(4-methylpiperazine-1-carbonyl)benzoic Acid → 1-(4-(6-((Dimethylamino)methyl)-4-morpholinopyrrolo[2,1-f][1,2,4]triazin-2-yl)phenyl)-3-(4-(4-methylpiperazine-1-carbonyl)phenyl)urea

https://huagongshe.com/reaction/63795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-methylpiperazine-1-carbonyl)benzoic AcidHCID 2051417—
ReactantHCID 117987912HCID 117987912—
ReactantHCID 117988374HCID 117988374—
Product1-(4-(6-((Dimethylamino)methyl)-4-morpholinopyrrolo[2,1-f][1,2,4]triazin-2-yl)phenyl)-3-(4-(4-methylpiperazine-1-carbonyl)phenyl)ureaHCID 7254910415.1%

Reaction Steps

According to the general methods described in example 13, 4-(4-methylpiperazine-1-carbonyl)benzoic acid was used as starting material, and the resulting 4-(4-methylpiperazine-1-carbonyl)benzoyl azide reacted with 13a to give a white solid (9 mg, 15.1%). 1H NMR (300 MHz, DMSO-d6): δ 9.63 (br, s, 2H), 8.16 (d, J=8.9 Hz, 2H), 7.92 (s, 1H), 7.57 (d, J=8.9 Hz, 2H), 7.53 (d, J=8.5 Hz, 2H), 7.34 (d, J=8.5 Hz, 2H), 7.13 (s, 1H), 4.07 (br, s, 6H), 3.80 (br, s, 4H), 3.51 (br, s, 4H), 3.06 (br s, 2H), 2.55 (s, 6H), 2.38 (br s, 2H), 2.24 (s, 3H). ESI-MS: 598 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447101B2
Source datasetuspto-grants-2016_09
ORD IDord-74cbe61f66974864af3f503e3f73580d
Source noteuspto-grants-2016_09